{(E)-1-[1-Hydroxy-meth-(E)-ylidene]-3-phenyl-allyl}-phosphonic acid diethyl ester

Base Information

• Chemical Name: {(E)-1-[1-Hydroxy-meth-(E)-ylidene]-3-phenyl-allyl}-phosphonic acid diethyl ester
• CAS No.: 173379-31-2
• Molecular Formula: C₁₄H₁₉O₄P
• Molecular Weight: 282.276
• Mol file: 173379-31-2.mol

Synonyms:{(E)-1-[1-Hydroxy-meth-(E)-ylidene]-3-phenyl-allyl}-phosphonic acid diethyl ester

Chemical Property of {(E)-1-[1-Hydroxy-meth-(E)-ylidene]-3-phenyl-allyl}-phosphonic acid diethyl ester

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
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MSDS Files:

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Technology Process of {(E)-1-[1-Hydroxy-meth-(E)-ylidene]-3-phenyl-allyl}-phosphonic acid diethyl ester

There total 1 articles about {(E)-1-[1-Hydroxy-meth-(E)-ylidene]-3-phenyl-allyl}-phosphonic acid diethyl ester which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

diethyl (E)-cinnamylphosphonate (52378-69-5) + formic acid ethyl ester (109-94-4) → {(E)-1-[1-Hydroxy-meth-(E)-ylidene]-3-phenyl-allyl}-phosphonic acid diethyl ester (173379-31-2)

Guidance literature:

With hydrogenchloride; n-butyllithium; diisopropylamine; In tetrahydrofuran; hexane; at -70 ℃; Yield given; 1.) 10 min; 2.) 30 min; 3.) pH=3;

DOI:10.1055/s-1995-4122

Reference yield: 88.0%

tert-butylchlorodiphenylsilane (58479-61-1) + {(E)-1-[1-Hydroxy-meth-(E)-ylidene]-3-phenyl-allyl}-phosphonic acid diethyl ester (173379-31-2) → {(E)-1-[1-(tert-Butyl-diphenyl-silanyloxy)-meth-(E)-ylidene]-3-phenyl-allyl}-phosphonic acid diethyl ester

Guidance literature:

With triethylamine; In diethyl ether; at 0 ℃; for 0.25h;

DOI:10.1055/s-1995-4122

Reference yield: 84.0%

acetyl chloride (75-36-5) + {(E)-1-[1-Hydroxy-meth-(E)-ylidene]-3-phenyl-allyl}-phosphonic acid diethyl ester (173379-31-2) → Acetic acid (1E,3E)-2-(diethoxy-phosphoryl)-4-phenyl-buta-1,3-dienyl ester

Guidance literature:

With triethylamine; In diethyl ether; at 0 ℃; for 0.25h;

DOI:10.1055/s-1995-4122

upstream raw materials:

diethyl (E)-cinnamylphosphonate

formic acid ethyl ester